Canonical Allele Identifier: CA31469872

Gene: KCNJ10

Linked Data

• dbSNP Id: rs762083144
• gnomAD v4: 1-160041322-G-C
• MyVariant Identifiers: chr1:g.160011112G>C (hg19) ; chr1:g.160041322G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041322G>C , CM000663.2:g.160041322G>C	GRCh38
NC_000001.10:g.160011112G>C , CM000663.1:g.160011112G>C	GRCh37
NC_000001.9:g.158277736G>C	NCBI36
NG_016411.1:g.33850C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+512C>G
ENST00000636689.1:n.95-1974C>G
ENST00000637644.1:c.487+724C>G	ENSP00000490282.1:n.487+724C>G
ENST00000638728.1:c.*71C>G	ENSP00000492619.1:n.*71C>G
ENST00000638840.1:c.919+14C>G
ENST00000638868.1:c.*71C>G	ENSP00000491250.1:n.*71C>G
ENST00000639408.1:c.488-721C>G	ENSP00000491635.1:n.488-721C>G
ENST00000640017.1:c.669+512C>G	ENSP00000491337.1:n.669+512C>G
ENST00000640914.1:c.124+512C>G
ENST00000644903.1:c.*71C>G MANE Select	ENSP00000495557.1:n.*71C>G
ENST00000368089.3:c.*71C>G	ENSP00000357068.3:n.*71C>G
ENST00000509700.1:n.462+512C>G
NM_002241.4:c.*71C>G	NP_002232.2:n.*71C>G
NM_002241.5:c.*71C>G MANE Select	NP_002232.2:n.*71C>G